FDA Inspection 947144 — Eckert & Ziegler Radiopharma GmbH

Eckert & Ziegler Radiopharma GmbH — FEI 3005746948

The FDA completed an inspection of Eckert & Ziegler Radiopharma GmbH on November 6, 2015 in Berlin. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
November 6, 2015
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Berlin (Germany)